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NeoNavia base unit

by Neonavia AB Sweden EUDAMED

Ref REF# 1102

EMDN A01020199

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number735008194NEONAVIAREUSEDE Basic UDI-DIDate6 Feb 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Reusable parts of biopsy system
Model / Reference
REF# 1102
Primary DI / UDI-DI
17350081940031
Basic UDI-DI
735008194NEONAVIAREUSEDE
Direct Marketing DI
17350081940031
EMDN Code
A01020199 Needles and kits for histological and cytological biopsy of soft tissues - other
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
SE-MF-000045971

Other devices from Neonavia AB

Properties & raw data

Show properties, registry sources and raw records
Other properties (13)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED ddb8b0f0-59b3-4a41-b398-a2c0576b1889 61 fields · synced 22 Oct 2026